advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 02-12-2015, 01:22 PM #14
IH8PN IH8PN is offline
Junior Member
 
Join Date: Feb 2014
Posts: 82
10 yr Member
IH8PN IH8PN is offline
Junior Member
 
Join Date: Feb 2014
Posts: 82
10 yr Member
Default

I hate to say it, but no my PN is not gone. I've stayed away from posting for 2 reasons. First is I'm not sure much has changed for me in the past few months. Second is I feel I'm better off mentally if I find ways to distract myself from my symptoms rather than dwell in them. Posting may bring some baggage with it as I bring to light all the things I hate about this disease. I'd much rather distract myself.

I can echo the sentiments of many when I say that some days I feel like I'm getting better, some days it feels worse, and other times I think I'm just getting used to it.

The PN in my feet is 95% related to pressure, meaning that the pain in the soles of my feet steadily worsens when standing and tapers off fairly quickly when I sit. The other 5% is random twitching, prickling, and feelings of coldness that seem to come and go on their own.

I have been pretty good about taking better care of myself the past 3 months. Diet has gotten better with more fruits and vegetables, exercise 3-4 times a week on the bicycle, alcohol and junk food way down, and still a steady dose of supplements. I haven't noticed a significant change in pain levels with or without the above, but I feel better mentally knowing that I'm taking care of myself.

Tried capsaicin the other day because at this point I'm willing to try anything. That was a bad idea. awful burning that started a few hours after application and didn't die off until 24 hrs later. I know there were warnings from others on here about capsaicin but I had to try it for myself. I'll never do that again for what its worth.

My neurologists sucks. I told him the gabapentin wasn't working and that I'd like to taper off and try something else. He wanted me to see how I felt without the gabapentin first. I'm sick of having to suggest ideas and beg for help. Shouldn't my MD be the one to offer suggestions and help? I'd like to get off medications anyway so I'm not going to stress about not being offered an alternative to try. My next course of action may be to try and get a hold of a compound cream if I were to try a new medication.
IH8PN is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Joe Duffer (02-13-2015), MissyJ (10-25-2015)
 


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Hi Everyone! My Story piratemet Thoracic Outlet Syndrome 0 01-12-2012 03:06 PM
Here is my story.... marykay1959 New Member Introductions 3 10-18-2010 02:04 AM
Social Security News: Powerful TV Story On Backlogs (VIDEO Story) Stitcher Parkinson's Disease 1 07-14-2008 10:55 AM


All times are GMT -5. The time now is 06:42 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.